MAUDE manufacturer profile

MEDTRONIC NEUROMODULATION · LNQ

MAUDE profile for Intestinal Stimulator

Key facts

Manufacturer MEDTRONIC NEUROMODULATION
Manufacturer group MEDTRONIC NEUROMODULATION
Product code LNQ
Product code name Intestinal Stimulator

At a glance

  • 100–999 MAUDE reports
  • 10–99 Death reports
  • 100–999 Injury reports
  • 100–999 Malfunction reports
  • 100–999 Problems flagged by Orca1 signal analytics
  • No Known Impact Or Consequence To Patient, Adverse Event Without Identified Device or Use Problem, Device Operates Differently Than Expected, Inappropriate/Inadequate Shock/Stimulation, Electric Shock, High impedance, Pain, Migration or Expulsion of Device Most reported problems

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About MAUDE manufacturer and product code profiles

Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.

Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1

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